To link zinc to adenylates
research highlights
Biocatalysis
To link zinc to adenylates
Commun. Biol. 1, 113 (2018).
Zinc is an essential micronutrient
that serves as an important enzymatic
co-factor in many biochemical reactions.
A deficiency in zinc can result in a
variety of health issues, ranging from
neurological deficits to immune
disorders to poor hepatic function.
Preliminary reports suggest a linkage
between adenylate, along with its
associated nucleotides (AMP, ADP, ATP),
and zinc metabolism. In a new report in
Communications Biology, four extra-cellular
enzymes involved in hydrolysis to the
ATP degradation products have been
related to the biochemistry of this
co-factor. By correlating metabolite
levels—in vitro and in vivo—with enzyme
activity levels of four extra-cellular
associated enzymes, investigators found a
link between zinc metabolism and levels
of adenine-associated metabolites.
This relationship varied by tissue,
which would be consistent with
expression levels of the associated
enzymes.
CN
https://doi.org/10.1038/s41684-018-0168-7
Osteoporosis
Boning up on turnover
Nat. Commun. 9, 3428 (2018).
Like most physiological phenomena,
bone status is a combination of creation
and degradation. In older adults these
processes become dysregulated and
are potential targets for therapy.
Amongst the proteins involved in the
anabolic processes that build bone are
bone morphogenetic proteins (BMPs).
A new study that explored these proteins
and their interaction with a ubiquitin
ligase, SMURF1, found that response to
interventions in mice and older adults
fell into different categories, based on
BMP-2 and SMURF1 response. After various
experiments, including altering SMURF1
protein levels and various pharmacological
interventions, there is room for clinical
improvement. Specifically, decreasing
levels of SMURF1 in osteoclasts—bone
generating cells—holds promise as a
therapeutic strategy amongst older,
osteoporotic individuals.
CN
https://doi.org/10.1038/s41684-018-0169-6
Ageing
Less methionine means
more health
Cell Rep. 24, 2392–2403 (2018).
Dietary modification as a method to improve
lifespan and/or healthspan is an area of much
interest. While there is a significant body of
literature establishing caloric restriction as
one method to increase longevity, much less
information is available on other strategies.
In Cell Reports, a new study describes a
methionine restricted diet that extends
lifespan in not only wildtype mice, but also
in a mouse model of Hutchinson-Gilford
Progeria Syndrome; a disease resembling
premature aging. Transcriptomic analysis of
hepatic tissues from both genotypes revealed
significant down regulation of inflammatory
pathways with methionine restriction, with
changes also present in DNA repair. Lipid
profiles changed as well between the control
and methionine restricted diet. Moreover,
addition of cholic acid to the diet improved
lifespan and healthspan in the progeria
mouse model.
CN
Lab Animal
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https://doi.org/10.1038/s41684-018-0170-0
Gene expression profiling
Standard Tip
Worms expressing
themselves
PLoS Genet. 14, e1007559 (2018)
Caenorhabditis elegans is the organism
of choice for exploring many biological
phenomena due to its small size, rapid
generation time, and well-described genome.
Despite the multitude of studies using this
worm as a model, little information was
available on the transcriptome of the four
tissues of adult worms—muscle, neuron,
intestine, and epidermis—versus those of
embryonic and larval stage animals. By
busting open worms and separating tissues,
investigators compared the expression
profiles of the four tissues with single cell
resolution. They identified mRNAs that
were ubiquitously expressed across all
tissues versus those that were enriched in
one. In addition, they also characterized
differences in alternative transcript splicing.
For example, authors observed differences in
ribosomal proteins and cytoskeletal proteins
in the different tissues.
CN
https://doi.org/10.1038/s41684-018-0171-z
Ellen P. Neff and Clark Nelson
Lab Animal | VOL 47 | OCTOBER 2018 | 267–272 | www.nature.com/laban
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